Article
Generation and characterization of a laforin nanobody inhibitor
2021-01-20
Abstract excerpt
Mutations in the gene encoding the glycogen phosphatase laforin result in the fatal childhood epilepsy Lafora disease (LD). A cellular hallmark of LD is cytoplasmic, hyper-phosphorylated, glycogen-like aggregates called Lafora bodies (LBs) that form in nearly all tissues and drive disease progression. Additional tools are needed to define the cellular function of laforin, understand the pathological role of lafori...
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Identifiers and source
- Literature Corpus work
- 54c30c18-e1a0-5155-af17-9eeeb0d60da8
- DOI
- 10.1101/2021.01.20.426524
